Clinical Research Coordinator - Part Time
New York, NYPart-time
Behavioral Health Market Context
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Benefits
Part-Time | One Day per Week (On-Site)One consistent day per week (on-site)Supplemental incomePortfolio or semi-retired workBalance alongside another research or clinical roleCompetitive hourly compensation commensurate with experienceA highly organized, collaborative, and respectful research environment4 more items(s)
Qualifications
- •Certified Clinical Research Coordinator (CCRC) required
- •Minimum 2+ years of hands-on clinical research coordination experience
- •Strong working knowledge of GCP, ICH, FDA regulations, and IRB processes
- •Experience working directly with sponsors, CROs, and monitors
- •Excellent organizational skills with high attention to detail
- •Professional, patient-centered communication style
- •Ability to work independently and efficiently in a focused, one-day-per-week role
- •The opportunity to contribute meaningfully to clinical research without a full-time commitment
- •Stable, predictable schedule with minimal administrative burden
- •6 more items(s)
Responsibilities
- •We are seeking a Certified Clinical Research Coordinator (CCRC) to join our growing clinical research site on a part-time basis (one day per week)
- •This role is ideal for an experienced coordinator who values high-quality research, operational excellence, and schedule flexibility
- •The CCRC will play a critical role in ensuring the ethical, regulatory, and operational integrity of clinical trials while supporting investigators, participants, and sponsors in a highly organized and patient-centered environment
- •Coordinate and manage assigned clinical trials in compliance with GCP, ICH, FDA regulations, and IRB requirements
- •Serve as the primary point of contact for study participants, investigators, sponsors, and CROs on assigned study days
- •Conduct study visits, including participant screening, informed consent, visit coordination, and protocol-specified procedures
- •Ensure accurate, timely, and complete documentation in source documents, EDC systems, and regulatory binders
- •Support monitoring visits, audits, and inspections, ensuring readiness and responsiveness
- •Maintain study supplies, investigational product accountability, and specimen handling per protocol
- •Collaborate closely with the Principal Investigator and research leadership to support study success
- •7 more items(s)
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